abnormality of citrulline metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of a metabolism or concentration of citrulline. (Human Phenotype Ontology, HP_0011965)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011965
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3 genes associated with the abnormality of citrulline metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CPS1 carbamoyl-phosphate synthase 1, mitochondrial
OTC ornithine carbamoyltransferase
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13